A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736698



Internal ID160364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:45103314..45103755hg38UCSC Ensembl
chrX:44962559..44963000hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg38442
hg19442
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5432591
Supporting Variants
Samples
Known GenesKDM6A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736698
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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